Rouleau GA - Search Results

1

Clinical and genetic study of hereditary spastic paraplegia in Canada.

Chrestian N, Dupré N, Gan-Or Z, Szuto A, Chen S, Venkitachalam A, Brisson JD, Warman-Chardon J, Ahmed S, Ashtiani S, MacDonald H, Mohsin N, Mourabit-Amari K, Provencher P, Boycott KM, Stavropoulos DJ, Dion PA, Ray PN, Suchowersky O, Rouleau GA, Yoon G. Chrestian N, et al. Among authors: rouleau ga. Neurol Genet. 2016 Dec 5;3(1):e122. doi: 10.1212/NXG.0000000000000122. eCollection 2017 Feb. Neurol Genet. 2016. PMID: 27957547 Free PMC article.

2

The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.

Howard HC, Mount DB, Rochefort D, Byun N, Dupré N, Lu J, Fan X, Song L, Rivière JB, Prévost C, Horst J, Simonati A, Lemcke B, Welch R, England R, Zhan FQ, Mercado A, Siesser WB, George AL Jr, McDonald MP, Bouchard JP, Mathieu J, Delpire E, Rouleau GA. Howard HC, et al. Among authors: rouleau ga. Nat Genet. 2002 Nov;32(3):384-92. doi: 10.1038/ng1002. Epub 2002 Oct 7. Nat Genet. 2002. PMID: 12368912

3

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.

Dupré N, Verlaan DJ, Hand CK, Laurent SB, Turecki G, Davenport WJ, Acciarri N, Dichgans J, Ohkuma A, Siegel AM, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Can J Neurol Sci. 2003 May;30(2):122-8. doi: 10.1017/s0317167100053385. Can J Neurol Sci. 2003. PMID: 12774951

4

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum.

Dupré N, Howard HC, Mathieu J, Karpati G, Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Ann Neurol. 2003 Jul;54(1):9-18. doi: 10.1002/ana.77777. Ann Neurol. 2003. PMID: 12838516 Review.

5

HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.

Fan X, Messaed C, Dion P, Laganiere J, Brais B, Karpati G, Rouleau GA. Fan X, et al. Among authors: rouleau ga. Can J Neurol Sci. 2003 Aug;30(3):244-51. doi: 10.1017/s0317167100002675. Can J Neurol Sci. 2003. PMID: 12945950

6

A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.

Meijer IA, Cossette P, Roussel J, Benard M, Toupin S, Rouleau GA. Meijer IA, et al. Among authors: rouleau ga. Ann Neurol. 2004 Oct;56(4):579-82. doi: 10.1002/ana.20239. Ann Neurol. 2004. PMID: 15455396

7

Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts.

Toulouse A, Au-Yeung F, Gaspar C, Roussel J, Dion P, Rouleau GA. Toulouse A, et al. Among authors: rouleau ga. Hum Mol Genet. 2005 Sep 15;14(18):2649-60. doi: 10.1093/hmg/ddi299. Epub 2005 Aug 8. Hum Mol Genet. 2005. PMID: 16087686

8

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population.

Dupré N, Bouchard JP, Brais B, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Can J Neurol Sci. 2006 May;33(2):149-57. doi: 10.1017/s031716710000490x. Can J Neurol Sci. 2006. PMID: 16736723 Review.

9

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.

Gros-Louis F, Dupré N, Dion P, Fox MA, Laurent S, Verreault S, Sanes JR, Bouchard JP, Rouleau GA. Gros-Louis F, et al. Among authors: rouleau ga. Nat Genet. 2007 Jan;39(1):80-5. doi: 10.1038/ng1927. Epub 2006 Dec 10. Nat Genet. 2007. PMID: 17159980

10

Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.

Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz M, Reid E, Dion PA, Drapeau P, Rouleau GA. Valdmanis PN, et al. Among authors: rouleau ga. Am J Hum Genet. 2007 Jan;80(1):152-61. doi: 10.1086/510782. Epub 2006 Dec 1. Am J Hum Genet. 2007. PMID: 17160902 Free PMC article.

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